ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15094498
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.186681619T>C
GRCh37
chr1:g.186650751T>C
Linked Data - Sequence & Population
gnomAD v2:
1:186650751 T / C
gnomAD v3:
1:186681619 T / C
gnomAD v4:
chr1-186681619-T-C
Joint Max Group AF
0.44916292 (EAS)
Genomes Max Group AF
0.44916292 (EAS)
Linked Data - NCBI & NCI
dbSNP:
689466
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.186681619T>C , CM000663.2:g.186681619T>C
GRCh38
NC_000001.10:g.186650751T>C , CM000663.1:g.186650751T>C
GRCh37
NC_000001.9:g.184917374T>C
NCBI36
NG_028206.2:g.3809A>G
Search 100 bp 5'
Search 100 bp 3'